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Definitions

• the present invention relates to substituted cyclohexyl-1,4-diamine compounds, processes for the production thereof, pharmaceutical compositions containing these compounds, methods of producing pharmaceutical compositions including these compounds and related methods of treating or inhibiting certain diseases or conditions.
• ⁇ -opioids such as morphine are very effective in the treatment of strong to very strong pain and are of great importance for the treatment of pain.
• further opioid receptors in particular the ORL1 receptor
• pure ⁇ -opioids also have undesirable side effects, such as obstipation and respiratory depression, and may also lead to addiction.
• the opioid receptors ⁇ , ⁇ and ORL1 are also involved in the state of pain (Opioids: Introduction, pp. 127-150, Further Opioid Receptors, 455-476 in: Analgesics—From Chemistry and Pharmacology to Clinical Application, Wiley VCH, 2002).
• the ORL1 receptor is also involved in the regulation of further physiological and pathophysiological processes. These include inter alia learning and memory formation (Manabe et al, Nature, 394, 1997, pp. 577-581), Hörconf [Hearing capacity] (Nishi et al, EMBO J., 16, 1997, pp. 1858-1864) and numerous further processes. In a synopsis by Calo et al (Br. J. Pharmacol., 129, 2000, 1261-1283) there is an overview of the indications or biological procedures, in which the ORL1 receptor plays a part or could highly probably play a part.
• analgesics stimulation and regulation of nutrient absorption, effect on ⁇ -agonists such as morphine, treatment of withdrawal symptoms, reduction of the addiction potential of opioids, anxiolysis, modulation of motor activity, memory disturbances, epilepsy; modulation of neurotransmitter release, in particular of glutamate, serotonin and dopamine, and therefore neurodegenerative diseases; influencing the cardiovascular system, triggering an erection, diuresis, anti-natriuresis, electrolyte balance, arterial blood pressure, water-retention disorders, intestinal motility (diarrhea), relaxation of the respiratory tract, micturation reflex (urinary incontinence).
• agonists and antagonists such as anoretics, analgesics (also when administered with opioids) or nootropics will also be discussed.
• An object of the present invention was to provide pharmaceutical compositions which act on the opioid receptor system and are thus suitable for pharmaceutical compositions, in particular for the treatment of the various diseases associated with this system according to the prior art and for use in the indications mentioned therein.
• the compounds are also intended to influence noradrenalin and serotonin re-uptake.
• the invention therefore relates to substituted cyclohexyl-1,4-diamine derivatives of general formula I,
• R 1 and R 2 independently of one another represent H; respectively saturated or unsaturated, branched or unbranched, singly or multiply substituted or unsubstituted C 1-5 alkyl; respectively singly or multiply substituted or unsubstituted C 3-8 -cycloalkyl; or respectively singly or multiply substituted or unsubstituted aryl, C 3-8 cycloalkyl or heteroaryl bound by C 1-3 alkyl;
• R 1 and R 2 together represent CH 2 CH 2 OCH 2 CH 2 , CH 2 CH 2 NR 10 CH 2 CH 2 or (CH 2 ) 3-6 ,
• R 10 represents H; respectively saturated or unsaturated, branched or unbranched, singly or multiply substituted or unsubstituted C 1-5 alkyl; respectively singly or multiply substituted or unsubstituted C 3-8 cycloalkyl; respectively singly or multiply substituted or unsubstituted aryl or heteroaryl; or respectively singly or multiply substituted or unsubstituted aryl, C 3-8 cycloalkyl or heteroaryl bound by C 1-3 alkyl; respectively substituted or unsubstituted C(O)phenyl, C(O)heteroaryl, C(O)C 1-5 alkyl;
• R 3 represents respectively saturated or unsaturated, branched or unbranched, singly or multiply substituted or unsubstituted C 1-5 alkyl; respectively singly or multiply substituted or unsubstituted C 3-8 cycloalkyl; respectively unsubstituted or singly or multiply substituted aryl or heteroaryl; respectively unsubstituted or singly or multiply substituted aryl, heteroaryl or C 3-8 cycloalkyl bound by a C 1-3 alkyl group;
• A represents unsubstituted or singly or multiply substituted heteroaryl
• R 4 represents unsubstituted or singly or multiply substituted heteroaryl or aryl, or an unsubstituted or singly or multiply substituted heteroaryl or aryl radical linked by a C 1-3 alkyl chain,
• the enantiomers, diastereomers, mixtures of the enantiomers or diastereomers or an individual enantiomer or diastereomer in the form of the racemate; the enantiomers, diastereomers, mixtures of the enantiomers or diastereomers or an individual enantiomer or diastereomer; the bases and/or salts of physiologically acceptable acids or cations.
• the compounds according to the invention exhibit good binding to the ⁇ receptor and the ORL1 receptor, but also to other opioid receptors. Surprisingly it has been found that the compounds are also good inhibitors of noradrenalin and serotonin re-uptake. They are therefore also suitable for treating depression and/or bulimia and/or anorexia and/or catalepsy and/or anxiolysis and/or increasing alertness and/or libido.
• C 1-5 alkyl and “C 1-3 alkyl” comprise, in the context of this invention, acyclic saturated or unsaturated hydrocarbon radicals, which may be branched or straight-chained and unsubstituted or singly or multiply substituted, with 1, 2, 3, 4 or 5 C atoms or 1, 2 or 3 C atoms, i.e. C 1-5 alkanyls, C 2-5 alkenyls and C 2-5 alkynyls or C 1-3 alkanyls, C 2-3 alkenyls and C 2-3 alkynyls.
• Alkenyls have at least one C—C double bond and alkynyls at least one C—C treble bond.
• Alkyl is advantageously selected from the group comprising methyl, ethyl, n-propyl, 2-propyl, n-butyl, iso-butyl, sec.-butyl, tert.-butyl, n-pentyl, iso-pentyl, neo-pentyl, ethylenyl (vinyl), ethynyl, propenyl (—CH 2 CH ⁇ CH 2 , —CH ⁇ CH—CH 3 , —C( ⁇ CH 2 )—CH 3 ), propynyl (—CH—C ⁇ CH, —C ⁇ C—CH 3 ), 1,1-dimethylethyl, 1,1-dimethylpropyl, butenyl, butinyl, pentenyl and pentynyl.
• cycloalkyl or “C 3-8 cycloalkyl” means cyclic hydrocarbons with 3, 4, 5, 6, 7 or 8 carbon atoms, wherein the hydrocarbons may be saturated or unsaturated (but not aromatic), unsubstituted or singly or multiply substituted.
• cycloalkyl the term also comprises saturated or unsaturated (but not aromatic) cycloalkyls, in which one or two carbon atoms are replaced by an S, N or O heteroatom.
• C 3-8 cycloalkyl is advantageously selected from the group comprising cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclopentenyl, cyclohexenyl, cycloheptenyl and cyclooctenyl, but also tetrahydropyranyl, dioxanyl, dioxolanyl, morpholinyl, piperidinyl, piperazinyl, pyrazolinonyl and pyrrolidinyl.
• (CH 2 ) 3-6 denotes —CH 2 —CH 2 —CH 2 —, —CH 2 —CH 2 —CH 2 —CH 2 —, —CH 2 —CH 2 —CH 2 —CH 2 — und CH 2 —CH 2 —CH 2 —CH 2 —CH 2 —CH 2 —CH 2 —.
• aryl denotes carbocyclic ring systems comprising at least one aromatic ring, but without a heteroatom in only one of the rings, inter alia phenyls, naphthyls and phenanthrenyls, fluoranthenyls, fluorenyls, indanyls and tetralinyls.
• the aryl radicals can also be condensed with further saturated, (partially) unsaturated or aromatic ring systems.
• Each aryl radical can be present unsubstituted or singly or multiply substituted, wherein the aryl substituents may be the same or different and in any desired and possible position of the aryl. Phenyl or naphthyl radicals are particularly advantageous.
• heteroaryl represents a 5-, 6- or 7-membered cyclic aromatic radical, which contains at least 1 heteroatom, optionally also 2, 3, 4 or 5 heteroatoms, wherein the heteroatoms may be the same or different and the heterocycle may be unsubstituted or singly or multiply substituted; in the case of substitution on the heterocycle, the substituents may be the same or different and in any desired and possible position of the heteroaryl.
• the heterocycle may also be part of a bi- or polycyclic system. Preferred heteroatoms are nitrogen, oxygen and sulphur.
• heteroaryl radical is selected from the group comprising pyrrolyl, indolyl, furyl (furanyl), benzofuranyl, thienyl (thiophenyl), benzothienyl, benzothiadiazolyl, benzothiazolyl, benzotriazolyl, benzodioxolanyl, benzodioxanyl, phthalazinyl, pyrazolyl, imidazolyl, thiazolyl, oxazolyl, isoxazoyl, pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl, pyranyl, indazolyl, purinyl, indolizinyl, quinolinyl, isoquinolinyl, isothiazolyl, imidazolyl, triazolyl, triazinyl, quinazolinyl, carbazolyl, phenazinyl, phen
• the term “substituted”, according to this invention, denotes substitution of one or more hydrogen radicals by F, CI, Br, I, —CN, ⁇ O, ⁇ S, NH 2 , NH-alkyl, NH-aryl, NH-heteroaryl, NH-cycloalkyl, NH-alkyl-aryl, NH-alkyl-heteroaryl, NH-alkyl-OH, N(alkyl) 2 , N(alkyl-aryl) 2 , N(alkyl-heteroaryl) 2 , N(cycloalkyl) 2 , N(alkyl-OH) 2 , NH(C ⁇ O)alkyl, NH(C ⁇ O)aryl, NO 2 , SH, S-alkyl, S-aryl, S-heteroaryl, S-alkyl-aryl, S-alkyl-heteroaryl, S-cycloalkyl, NH 2 , S
• a substituent may optionally also be substituted for its part; thus —O-alkyl also includes inter alia —O—CH 2 —CH 2 —O—CH 2 —CH 2 —OH.
• aryl “heteroaryl” and “cycloalkyl”, according to this invention, “singly or multiply substituted” denotes the single or multiple, for example double, treble, quadruple or quintuple, substitution of one or more hydrogen atoms of the ring system by F, CI, Br, I, CN, NH 2 , NH-alkyl, NH-aryl, NH-heteroaryl, NH-alkyl-aryl, NH-alkyl-heteroaryl, NH-cycloalkyl, NH-alkyl-OH, N(alkyl) 2 , N(alkyl-aryl) 2 , N(alkyl-heteroaryl) 2 , N(cycloalkyl) 2 , N(alkyl-OH) 2 , NO 2 , SH, S-alkyl, S-cycloalkyl, S-aryl, S-heteroaryl, S-alkyl-alkyl
• salt denotes any form of the active ingredient according to this invention in which it assumes or is charged with an ionic form and is coupled to a counter ion (a cation or anion) or is in solution.
• This also includes complexes of the active ingredient with other molecules and ions, in particular complexes complexed by ionic interactions.
• physiologically acceptable salts in particular physiologically acceptable salts with cations or bases and physiologically acceptable salts with anions or acids or else a salt formed with a physiologically acceptable acid or physiologically acceptable cation.
• physiologically acceptable salt with anions or acids denotes, in the context of this invention, salts of at least one of the compounds according to this invention—usually protonated, for example on nitrogen—as a cation with at least one anion which are physiologically acceptable—in particular when applied to humans and/or mammals.
• this denotes, in particular, the salt formed with a physiologically acceptable acid, namely salts of the respective active ingredient with inorganic or organic acids which are physiologically acceptable—in particular when applied to humans and/or mammals.
• physiologically acceptable salts of specific acids include salts of: hydrochloric acid, hydrobromic acid, sulphuric acid, methane sulphonic acid, formic acid, acetic acid, oxalic acid, succinic acid, malic acid, tartaric acid, mandelic acid, fumaric acid, lactic acid, citric acid, glutamic acid, saccharic acid, monomethyl sebacic acid, 5-oxo-proline, hexane-1-sulphonic acid, nicotinic acid, 2-, 3- or 4-amino benzoic acid, 2,4,6-trimethyl-benzoic acid, ⁇ -lipoic acid, acetyl glycine, phosphoric acid, maleic acid, malonic acid, hippuric acid and/or aspartic acid.
• the hydrochloride salt, the citrate and the hemicitrate are particularly preferred.
• salt formed with a physiologically acceptable acid denotes salts of the respective active ingredient with inorganic or organic acids which are physiologically acceptable—in particular when applied to humans and/or mammals.
• the hydrochloride and the citrate are particularly preferred.
• physiologically acceptable acids include: hydrochloric acid, hydrobromic acid, sulphuric acid, methane sulphonic acid, formic acid, acetic acid, oxalic acid, succinic acid, tartaric acid, mandelic acid, fumaric acid, lactic acid, citric acid, glutamic acid, saccharic acid, monomethyl sebacic acid, 5-oxo-proline, hexane-1-sulphonic acid, nicotinic acid, 2-, 3- or 4-amino benzoic acid, 2,4,6-trimethyl-benzoic acid, ⁇ -lipoic acid, acetyl glycine, hippuric acid and/or aspartic acid.
• physiologically acceptable salt with cations or bases denotes, in the context of this invention, salts of at least one of the compounds according to this invention—usually a (deprotonated) acid—as an anion with at least one, preferably inorganic, cation, which are physiologically acceptable, in particular when applied to humans and/or mammals.
• the salts of the alkali and alkaline-earth metals are particularly preferred, but also ammonium salts, in particular (mono-) or (di-) sodium, (mono-) or (di-)potassium, magnesium or calcium salts.
• salt formed with a physiologically acceptable cation denotes, according to this invention, salts of at least one of the respective compounds as an anion with at least one inorganic cation, which are physiologically acceptable, in particular when applied to humans and/or mammals.
• the salts of the alkali and alkaline-earth metals are particularly preferred, but also ammonium salts, in particular (mono-) or (di-)sodium, (mono-) or (di-)potassium, magnesium or calcium salts.
• R 1 and R 2 independently of one another represent H; saturated or unsaturated, branched or unbranched, singly or multiply substituted or unsubstituted C 1-5 alkyl;
• radicals R 1 and R 2 together form a ring and represent CH 2 CH 2 OCH 2 CH 2 , CH 2 CH 2 NR 10 CH 2 CH 2 or (CH 2 ) 3-6 ,
• R 10 represents H; saturated or unsaturated, branched or unbranched, singly or multiply substituted or unsubstituted C 1-5 alkyl.
• R 1 and R 2 independently of one another represent CH 3 or H, wherein R 1 and R 2 do not simultaneously represent H, or R 1 and R 2 represent CH 2 CH 2 OCH 2 CH 2 , (CH 2 ) 4 , (CH 2 ) 5 or (CH 2 ) 6 .
• substituted cyclohexyl-1,4-diamine derivatives wherein R 3 represents respectively unsubstituted or singly or multiply substituted cyclopentyl, cyclohexyl, phenyl, benzyl, naphthyl, anthracenyl, thiophenyl, benzothiophenyl, furyl, benzofuranyl, benzodioxolanyl, indolyl, indanyl, benzodioxanyl, pyrrolyl, pyridyl, pyrimidyl or pyrazinyl; respectively unsubstituted or singly or multiply substituted C 5-6 cycloalkyl, phenyl, naphthyl, anthracenyl, thiophenyl, benzothiophenyl, pyridyl, furyl, benzofuranyl, benzodioxolanyl, indolyl, indanyl
• R 3 represents respectively unsubstituted or singly or multiply substituted phenyl, furyl, thiophenyl, naphthyl, benzyl, benzofuranyl, indolyl, indanyl, benzodioxanyl, benzodioxanyl, pyridyl, pyrimidyl, pyrazinyl or benzothiophenyl; respectively unsubstituted or singly or multiply substituted phenyl, furyl or thiophenyl bound by a saturated, unbranched C 1-2 alkyl group.
• R 3 represents respectively substituted or unsubstituted phenyl, phenethyl, thiophenyl, pyridyl or benzyl, particularly preferably 4-methylbenzyl, 2-methylbenzyl, 3-chlorobenzyl, 4-chlorobenzyl, 2-chlorobenzyl, 4-fluorobenzyl, 3-fluorobenzyl, 3-methylbenzyl, 2-fluorobenzyl, benzyl, phenethyl, phenyl, pyridyl, thiophenyl and 3-fluorophenyl.
• substituted cyclohexyl-1,4-diamine derivatives wherein A represents unsubstituted or singly or multiply substituted pyrrolyl, thiophenyl, furanyl, pyrazolyl, isoxazolyl, oxazolyl, isothiazolyl, imidazolyl, triazolyl, tetrahydroisoxazolyl, pyridinyl, pyrimidinyl, pyrazinyl, triazinyl, indolyl, benzofuranyl, benzothiophenyl, indazolyl, benzimidazolyl, purinyl, quinolinyl, isoquinolinyl, phthalazine, benzothiadiazolyl, benzothiazolyl, benzotriazolyl, benzodioxolanyl, benzodioxanyl and carbazolyl.
• substituted cyclohexyl-1,4-diamine derivatives wherein A represents pyridyl, thiophenyl, pyrazolyl, triazolyl, tetrahydroisoxazolyl, isoxazolyl, thiazolyl and furanyl.
• substituted cyclohexyl-1,4-diamine derivatives wherein R 4 represents respectively unsubstituted or singly or multiply substituted phenyl, benzyl, naphthyl, anthracenyl, thiophenyl, benzothiophenyl, furanyl, isothiazolyl, imidazolyl, triazolyl, triazinyl, pyrazolyl, benzofuranyl, benzodioxolanyl, isoquinolinyl, phthalazine, benzo[1,2,5]thiadiazole, benzothiazole, benzotriazole, quinolinyl, carbazole, isoxazolyl, oxazolyl, indolyl, indanyl, benzodioxanyl, indazolyl, benzimidazolyl, pyrrolyl, pyridyl, pyrimidyl or pyrazinyl; respectively un
• R 4 represents respectively unsubstituted or singly or multiply substituted phenyl, benzyl, naphthyl, thiophenyl, benzothiophenyl, furanyl, isothiazolyl, imidazolyl, triazolyl, pyrazolyl, benzofuranyl, isoquinolinyl, benzothiazole, benzotriazole, quinolinyl, isoxazolyl, oxazolyl, indolyl, pyrrolyl, pyridyl, pyrimidyl or pyrazinyl; respectively unsubstituted or singly or multiply substituted benzyl or phenethyl.
• R 4 represents unsubstituted or singly or multiply substituted phenyl, pyrazolyl or thiophenyl.
• substituted cyclohexyl-1,4-diamine derivatives from the group comprising
• the enantiomers, diastereomers, mixtures of the enantiomers or diastereomers or an individual enantiomer or diastereomer in the form of the racemate; the enantiomers, diastereomers, mixtures of the enantiomers or diastereomers or an individual enantiomer or diastereomer; the bases and/or salts of physiologically acceptable acids or cations.
• the substances according to the invention act, for example, on the ORL1 receptor that is relevant in connection with various diseases, so they are suitable as a pharmaceutical active ingredient in a pharmaceutical composition.
• the invention therefore also relates to pharmaceutical preparations containing at least one substituted cyclohexyl carboxylic acid derivative according to the invention, and optionally suitable additives and/or auxiliaries and/or optionally further active ingredients.
• the pharmaceutical preparations according to the invention contain, in addition to at least one substituted cyclohexyl-1,4-diamine derivative according to the invention, optionally suitable additives and/or auxiliaries, therefore also excipients, fillers, solvents, diluents, dyes and/or binders and can be administered as liquid pharmaceutical preparations in the form of injection solutions, drops or syrups, as semi-solid pharmaceutical preparations in the form of granules, tablets, pellets, patches, capsules, plasters or aerosols.
• auxiliaries etc.
• compositions depend on whether the pharmaceutical preparation is to be applied orally, perorally, parenterally, intravenously, intraperitoneally, intradermally, intramuscularly, intranasally, buccally, rectally or topically, for example to the skin, the mucous membranes or the eyes.
• Preparations in the form of tablets, dragees, capsules, granules, drops, juices and syrups are suitable for oral application, solutions, suspensions, easily reconstitutable dry preparations and sprays are suitable for parenteral, topical and inhalative applications.
• Substituted cyclohexyl-1,4-diamine derivatives according to the invention in a deposit, in dissolved form or in a plaster, optionally with the addition of agents to promote skin penetration, are suitable percutaneous application preparations. Orally or percutaneously applicable preparation forms can release the substituted cyclohexyl-1,4-diamine derivatives according to the invention after a delay.
• the substituted cyclohexyl-1,4-diamine derivatives according to the invention may also be applied in the form of parenteral long-acting repositories such as implants or implanted pumps. In principle, further active ingredients known to the person skilled in the art can be added to the pharmaceutical preparations according to the invention.
• the amount of active ingredient to be administered to the patient varies as a function of the weight of the patient, the method of application, the indication and the severity of the illness. Conventionally, 0.00005 to 50 mg/kg, preferably 0.01 to 5 mg/kg, of at least one substituted cyclohexyl-1,4-diamine derivative according to the invention are applied.
• the pharmaceutical composition contains a further active ingredient, in particular an opioid, preferably a strong opioid, in particular morphine, or an anaesthetic, preferably hexobarbital or halothane.
• an opioid preferably a strong opioid, in particular morphine, or an anaesthetic, preferably hexobarbital or halothane.
• a contained substituted cyclohexyl-1,4-diamine derivative according to the invention is in the form of a pure diastereomer and/or enantiomer, as a racemate or as a non-equimolar or equimolar blend of the diastereomers and/or enantiomers.
• substituted cyclohexyl-1,4-diamine derivatives according to the invention can be used for producing a pharmaceutical composition for treating pain, in particular acute, neuropathic or chronic pain.
• the invention therefore also relates to the use of a substituted cyclohexyl-1,4-diamine derivative according to the invention for producing a pharmaceutical composition for treating pain, in particular acute, visceral, neuropathic or chronic pain.
• the invention also relates to the use of a substituted cyclohexyl-1,4-diamine derivative according to the invention for the production of a pharmaceutical composition for the treatment of anxiety, stress and stress-related syndromes, depression, epilepsy, Alzheimer's disease, senile dementia, general cognitive dysfunction, learning and memory disorders (as a nootropic), withdrawal symptoms, alcohol- and/or drug- and/or medicine abuse and/or dependency, sexual dysfunction, cardiovascular diseases, hypotension, hypertension, tinnitus, pruritus, migraine, hearing difficulties, deficient intestine motility, impaired absorption of nutrients, anorexia, obesity, locomotive disturbances, diarrhea, cachexia, urinary incontinence, or as a muscle relaxant, anti-convulsive or anaesthetic or for co-administration in treatment with an opioid analgesic or anaesthetic, for diuresis or anti-natriuresis, anxiolysis, for modulation of motor activity, for modulation of neurotransmitter release and treatment of neuro
• a substituted cyclohexyl-1,4-diamine derivative used is in the form of a pure diastereomer and/or enantiomer, as a racemate or as a non-equimolar or equimolar blend of the diastereomers and/or enantiomers.
• the invention also relates to a process for the treatment, in particular in one of the above-mentioned indications, of a non-human mammal or human, which or who requires treatment of pain, in particular chronic pain, by administration of a therapeutically effective dose of a substituted cyclohexyl-1,4-diamine derivative according to the invention, or of a pharmaceutical composition according to the invention.
• the invention also relates to a process for producing the substituted cyclohexyl-1,4-diamine derivatives according to the invention, as stated in the following description and examples.
• radicals R 01 and R 02 have the meaning given for compounds according to the invention of Formula I for R 1 and R 2 and, in addition, independently of one another can represent a protecting group.
• the remaining radicals have the meaning indicated in formula I:
• the process according to the invention is based on linking substituted cyclohexane-1,4-diamines, the production of which is known from the literature (WO 02090317), with anhydrides, carboxylic acids or preferably the activated analogues thereof, in particular acid halides or active esters thereof, and thus to convert them into compounds according to the invention.
• the reactions with anhydrides preferably take place in polar or non-polar aprotic solvents such as DMF, DMSO, diethylether, diusopropylether, THF, toluene, dichloromethane or acetonitrile at temperatures between ⁇ 20 and +110° C., preferably between ⁇ 10 and +40° C.
• polar or non-polar aprotic solvents such as DMF, DMSO, diethylether, diusopropylether, THF, toluene, dichloromethane or acetonitrile
• polar or non-polar aprotic solvents to which an organic or inorganic auxiliary base, preferably tertiary amines such as triethylamine, diisopropylethylamine or DMAP, has been added, are also used.
• auxiliary base preferably tertiary amines such as triethylamine, diisopropylethylamine or DMAP
• pyridine for example, is also suitable as a base and as a solvent.
• acid chlorides are reacted with amines at between ⁇ 10 and +40° C. in dichloromethane or chloroform in the presence of triethylamine or pyridine and optionally catalytic amounts of DMAP.
• the protecting groups are optionally then split off.
• ether means diethylether, “EE” ethylacetate and “DCM” dichloromethane.
• equivalents means amount of substance equivalents, “mp.” melting point or melting range, “decomp.” decomposition, “RT” room temperature, “abs.” absolute (anhydrous), “rac.” racemic, “conc.” concentrated, “min” minutes, “h” hours, “d” days, “vol.%” volume percent, “m %” mass percent and “M” is an indication of concentration in mol/l.
• Example Carboxylic acid used Name of example compound 1 5-methyl-2-phenyl-2H-[1,2,3]triazole-4- carboxylic acid (4-dimethylamino-4-phenyl- cyclohexyl)-amide 2 1-phenyl-5-propyl-1H-pyrazole-4-carboxylic acid [4-dimethylamino-4-(3-fluoro-phenyl)- cyclohexyl]-amide 3 3-(2,6-dichloro-phenyl)-5-methyl-isoxazole-4- carboxylic acid (4-benzyl-4-pyrrolidin-1-yl- cyclohexyl)-amide 4 5-methyl-2-phenyl-2H-[1,2,3]triazole-4- carboxylic acid (4-benzyl-4-piperidin-1-yl- cyclohexyl)-amide 5 5-methyl-2-phenyl-2-phenyl-2H-[1,2,3]triazole-4- carboxylic acid (4-
• the non-polar diastereoisomer of 1-(3-fluorophenyl)-N,N-dimethylcyclohexane-1,4-diamine (350 mg) was placed with 220 ⁇ I triethylamine (1.05 molar equivalents) and catalytic amounts of DMAP (about 5 mg) in 3.5 ml dichloromethane, 400 mg 3-(2-chlorophenyl)-5-methylisoxazole-4-carbonylchloride (1.05 molar equivalents), dissolved in 2 ml dichloromethane, were added dropwise at ⁇ 10° C. to and the mixture was stirred overnight while being heated to room temperature.
• the mixture was made alkaline (pH>10) with 2-molar sodium hydroxide solution, with ice cooling, the organic phase was separated, the aqueous phase extracted with dichloromethane (20 ml) and the combined organic phases dried over sodium sulphate, filtered and evaporated to dryness.
• Example 118 the polar diastereoisomer of 1-(3-fluorophenyl)-N,N-dimethylcyclohexane-1,4-diamine (350 mg) was reacted with 400 mg 3-(2-chlorophenyl)-5-methylisoxazole-4-carbonylchloride and worked up in a similar manner.
• Example 120 As described for Example 120, 238 mg of the polar diastereoisomer of 5-methyl-2-phenyl-2H-[1,2,3]triazole-4-carboxylic acid (4-dimethylamino-4-phenylcyclohexyl)amide were also obtained, which, dissolved in 5 ml 2-butanone and 5 ml ethyl acetate, were converted into the corresponding hydrochloride by adding 10.6 ⁇ l water, 75 ⁇ l chlorotrimethylsilane and 10 ml diisopropylether (165 mg of white solid).
• Example 120 700 mg of a cis-trans mixture of 1-(3-fluorophenyl)-N,N-dimethylcyclohexane-1,4-diamine were reacted with 810 mg 3-(2,6-dichlorophenyl)-5-methylisoxazole-4-carboxylic acid (1 molar equivalent) and the crude product (1.86 g) was isolated.
• Example 122 448 mg of the polar diastereoisomer of 3-(2,6-dichlorophenyl)-5-methylisoxazole-4-carboxylic-acid [4-dimethylamino-4-(3-fluorophenyl)cyclohexyl]amide were obtained, which, dissolved in 15 ml 2-butanone, 15 ml ethyl acetate and 2 ml methanol, were converted into the corresponding hydrochloride by adding 16.5 ⁇ l water, 116 ⁇ l chlorotrimethylsilane and 25 ml diusopropylether (364 mg of white solid, Mp. 246-248° C.).
• Example 120 As described for Example 120, 650 mg of a cis-trans mixture of N,N-dimethyl-1-phenlcyclohexane-1,4-diamine were reacted with 810 mg 3-(2,6-dichlorophenyl)-5-methylisoxazole-4-carboxylic acid (1 molar equivalent) and the crude product (1.92 g) was isolated.
• Example 124 341 mg of the polar diastereoisomer of 3-(2,6-dichlorophenyl)-5-methylisoxazole-4-carboxylic acid (4-dimethyl-amino-4-phenylcyclohexyl)amide were obtained, which, dissolved in 10 ml 2-butanone, 10 ml ethyl acetate and 2 ml methanol, were converted into the corresponding hydrochloride at 0° C. by adding 13 ⁇ l water, 92 ⁇ l chlorotrimethylsilane und 25 ml diisopropylether (292 mg of white solid).
• Example 120 700 mg of a cis-trans mixture of 1-(3-fluorophenyl)-N,N-dimethylcyclohexane-1,4-diamine were reacted with 600 mg 5-methyl-3-phenylisoxazole-4-carboxylic acid (1 molar equivalent) and the crude product was isolated.
• Example 120 As described for Example 120, 650 mg of a cis-trans mixture of N,N-dimethyl-1-phenylcyclohexane-1,4-diamine were reacted with 600 mg 5-methyl-3-phenylisoxazole-4-carboxylic acid (1 molar equivalent) and the crude product was isolated.
• Example 127 190 mg of the polar diastereoisomer of 5-methyl-3-phenylisoxazole-4-carboxylic acid (4-dimethylamino-4-phenylcyclohexyl)amide were also obtained, which, dissolved in 10 ml 2-butanone and 5 ml ethyl acetate, were converted into the corresponding hydrochloride by adding 8.5 ⁇ l water, 60 ⁇ l chlorotrimethylsilane and 10 ml diisopropylether (135 mg of white solid, Mp. 243-245° C.).
• the cyclohexane derivatives of general formula I were examined in a receptor binding assay with 3H-nociceptin/orphanin FQ with membranes of recombinant CHO-ORL1 cells.
• This test system was carried out according to the methods presented by Ardati et al (Mol. Pharmacol., 51, 1997, pp. 816-824).
• the concentration of 3H-nociceptin/orphanin FQ was 0.5 nM in these tests.
• the binding assays were carried out with 20 ⁇ g membrane protein per 200 ⁇ l batch in 50 mM Hepes, pH 7.4, 10 mM MgCl2 and 1 mM EDTA.
• the binding with the ORL1 receptor was determined by using 1 mg WGA-SPA beads (Amersham-Pharmacia, Freiburg), by incubation of the batch for one hour at RT and subsequent measurement in the Trilux scintillation counter (Wallac, Finland).
• the receptor affinity for human ⁇ -opiate receptor was determined in a homogenous batch in microtitre plates.
• dilution series of the respective substituted cyclohexyl-1,4-diamine derivative to be tested were incubated with a receptor membrane preparation (15-40 ⁇ g protein per 250 ⁇ l incubation batch) of CHO-K1 cells, which express the human ⁇ -opiate receptor (RB-HOM receptor membrane preparation from NEN, Zaventem, Belgium) in the presence of 1 nmol/l of the radioactive ligand [ 3 H]-naloxone (NET719, NEN, Zaventem, Belgium) and 1 mg WGA-SPA beads (wheat germ agglutinin SPA beads from Amersham/Pharmacia, Freiburg, Germany) in a total volume of 250 ⁇ l for 90 minutes at room temperature.
• IC 50 inhibition concentrations which bring about a 50% displacement of the radioactive ligand, were partially calculated by taking as a basis the percentage displacement by various concentrations of the compounds of general formula I to be tested. Ki values for the test substances were obtained as a result of conversion by means of the Cheng-Prusoff equation.

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